Device recall
Z-1582-2010: Stryker Orthopaedics, Scorpio Ceramic 4:1 Guide Size 13; XCelerate cutting block…
FDA device recall · Class II · Stryker Howmedica Osteonics Corp.
Key facts
| Recall number (Z-number) | Z-1582-2010 |
|---|---|
| Recall event | 54083 |
| Product | Stryker Orthopaedics, Scorpio Ceramic 4:1 Guide Size 13; XCelerate cutting block for distal femur in orthopaedic surgery, Non Sterile |
| Product code | LXH |
| Recalling firm | Stryker Howmedica Osteonics Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 14, 2012 |
| FEI number | 3003070421 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database